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EGFR c.707G>T ;(p.C236F)
Variant ID: 7-55220317-G-T
NM_005228.3(
EGFR
):c.707G>T;(p.C236F)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Identification of pathogenic missense mutations using protein stability predictors.
Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21
Variant appearance in text: EGFR: C236F
PubMed Link:
32958805
Variant Present in the following documents:
41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page
Advances in dynamic modeling of colorectal cancer signaling-network regions, a path toward targeted therapies.
Oncotarget
Tortolina, Lorenzo L; Duffy, David J DJ; Maffei, Massimo M; Castagnino, Nicoletta N; Carmody, Aimée M AM; Kolch, Walter W; Kholodenko, Boris N BN; De Ambrosi, Cristina C; Barla, Annalisa A; Biganzoli, Elia M EM; Nencioni, Alessio A; Patrone, Franco F; Ballestrero, Alberto A; Zoppoli, Gabriele G; Verri, Alessandro A; Parodi, Silvio S
Publication Date: 2015-03-10
Variant appearance in text: EGFR: c236f
PubMed Link:
25671297
Variant Present in the following documents:
oncotarget-06-5041-s001.pdf
View BVdb publication page
Mutant p53 in cancer: new functions and therapeutic opportunities.
Cancer Cell
Muller, Patricia A J PA; Vousden, Karen H KH
Publication Date: 2014-03-17
Variant appearance in text: EGFR: C236F
PubMed Link:
24651012
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page